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Taking people in PakistanNo phase

Training one arm versus both arms to recover hand and arm function after stroke

Compares one-arm and two-arm task training for arm recovery in people after stroke.

Plain-language title generated from the registry record
Registry title: Unilateral Versus Bilateral Task-specific Training on Motor Impairment, Upper Extremity Function, and Hand Dexterity in Post-Stroke Rehabilitation

Key facts

Where
Kot Addu, PakistanSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adults aged 40 to 75 who had a stroke 6 to 24 months ago, can lift the affected arm at the shoulder against gravity, and are medically stable.

Age
40 to 75 years
Sex
All sexes
Disease stage
Stroke diagnosed by a doctor (no more than three strokes in a lifetime), 6 to 24 months ago. Able to lift the weak arm at the shoulder against gravity.
Biomarker or test result
Abbreviated Mental Test score of 7 or more.

Main reasons for not taking part

  • Uncontrolled health conditions, such as unstable heart conditions
  • Major bone or joint problems in the affected arm
  • Hearing problems
  • Allergy to electrodes
  • Severe joint stiffness (contracture) that limits the needed arm movements

Read by machine on 13 November 2026.

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 40 and 75 years old?

Source: NCT07523503, who can take part

Where in Pakistan

  • HospitalsKot Addu, PakistanContact: Dr Izza Ayub Principal InvestigatorTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
University of Faisalabad
Trial code
NCT07523503
Record updated
13 April 2026
Original description
This randomized clinical trial will examine upper limb rehabilitation in individuals recovering from stroke. The study will compare unilateral and bilateral task-oriented training approaches to determine their relative effectiveness. Thirty-two medically stable participants with active shoulder movement and adequate cognition will be enrolled into two groups. Both groups will receive structured training for four weeks. Outcomes related to motor function and dexterity will be measured using standardized assessment tools. The aim is to identify the more effective strategy for improving upper extremity function after stroke.Read full original descriptionShow less

Unilateral Versus Bilateral Task-specific Training on Motor Impairment, Upper Extremity Function, and Hand Dexterity in Post-Stroke Rehabilitation

This randomized clinical trial will examine upper limb rehabilitation in individuals recovering from stroke. The study will compare unilateral and bilateral task-oriented training approaches to determine their relative effectiveness. Thirty-two medically stable participants with active shoulder movement and adequate cognition will be enrolled into two groups. Both groups will receive structured training for four weeks. Outcomes related to motor function and dexterity will be measured using standardized assessment tools. The aim is to identify the more effective strategy for improving upper extremity function after stroke.

Inclusion: • Age between 40 and 75 years; Clinically diagnosed stroke (no more than three lifetime episodes); Stroke duration between 6 to 24 months; Ability to perform antigravity shoulder movement with the paretic limb; Abbreviated Mental Test score ≥ 7; Medically stable and capable of giving consent.

Exclusion: • Uncontrolled systemic conditions (e.g. Unstable cardiac conditions); Major orthopedic issues affecting the involved upper limb; Hearing deficits; Allergy to electrodes; Receptive aphasia or severe language impairment; Severe joint contracture limiting required upper limb movements.

ClinicalTrials.gov NCT07523503